PAHs in PM2.5 in Zhengzhou: concentration,carcinogenic risk analysis,and source apportionment

Ambient air samples were collected at two different locations between 2011 and 2012 in Zhengzhou, China in order to assess the concentration level, health risks, as well as the sources of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM_2.5). The mean annual levels of PM_2.5 observed at industry site and residential site were 172?±?121 and 160?±?72 μg m^?3, respectively, which were about five times the annual value of proposed PM_2.5 standard (35 μg m^?3) in China. The PM_2.5 in all daily samples (n?=?47) exceeds the proposed PM_2.5 standard in China (75 μg m^?3) at both industrial and residential sites. Seasonal variations of PM_2.5 showed a clear trend of winter?>?autumn?>?spring?>?summer at both sites. The total concentrations of 16 PM_2.5-associated PAHs ranged from 61?±?51 to 431?±?281 and 38?±?25 to 254?±?189 ng m^?3, with mean value of 176?±?233 and 111?±?146 ng m^?3 at industry and residential sites, respectively. The major species were fluoranthene, pyrene, chrysene, benzo[b]fluoranthene and benzo[k]fluoranthene, and the concentration levels of PAHs in PM_2.5 were higher in winter than those of other seasons at both sites. The annual mean values of toxicity equivalency concentrations of ∑₁₆PAHs in PM_2.5 were 22.8 and 13.5 ng m^?3 in industry and residential area, respectively. In this study, the risk level of adult citizens through inhalation exposure to PAHs was calculated. The average estimates of lifetime inhalation cancer risks were approximately 8.9?×?10^?7 and 6.3?×?10^?7 for industry and residential sites, respectively. The main sources of 16 PAHs from both diagnostic ratios and principle component analysis identified as vehicular emissions and coal combustion.     

Characterization of As and trace metals embedded in PM10 particles in Puebla City, México

Forty-eight air-filter samples (PM₁₀) were analysed to identify the concentration level of partially leached metals (PLMs; As, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and V) from Puebla City, México. Samples were collected during 2008 from four monitoring sites: (1) Tecnológico (TEC), (2) Ninfas (NIN), (3) Hermanos Serdán (HS) and (4) Agua Santa (AS). The results indicate that in TEC, As (avg. 424 ng m^?3), V (avg. 19.2 ng m^?3), Fe (avg. 1,202 ng m^?3), Cu (avg. 86.6 ng m^?3), Cr (41.9 ng m^?3) and Ni (18.6 ng m^?3) are on the higher side than other populated regions around the world. The enrichment of PLMs is due to the industrial complexes generating huge dust particles involving various operations. The results are supported by the correlation of metals (Mn, Cd and Co) with Fe indicating its anthropogenic origin and likewise, As with Cd, Co, Fe, Mn, Pb and V. The separate cluster of As, Fe and Mn clearly signifies that it is due to continuous eruption of fumaroles from the active volcano Popocatépetl in the region.     

Contributions of dry and wet depositions of polychlorinated dibenzo-p-dioxins and dibenzofurans to a contaminated site resulting from a penetachlorophenol manufacturing process

The soils at a factory for manufacturing pentachlorophenol were heavily contaminated by polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). In order to verify the contributions of dry and wet deposition of PCDD/Fs from the ambient air, the concentration of PCDD/Fs in ambient air and soil were measured, the partition of particle- and gas-phases of atmospheric PCDD/Fs was calculated, and the annual fluxes of total dry and wet PCDD/F depositions were modeled. Average atmospheric PCDD/F concentration was 1.24 ng Nm^???3 (or 0.0397 ng I-TEQ Nm^???3). Moreover, over 92.8% of total PCDD/Fs were in the particle phase, and the dominant species were high chlorinated congeners. The total PCDD/F fluxes of dry and wet deposition were 119.5 ng m^???2 year^???1 (1.34 ng I-TEQ m^???2 year^???1) and 82.0 ng m^???2 year^???1 (1.07 ng I-TEQ m^???2 year^???1), respectively. By scenario simulation, the total fluxes of dry and wet PCDD/F depositions were 87.1 and 68.6 ng I-TEQ, respectively. However, the estimated PCDD/F contents in the contaminated soil were 839.9 ?? g I-TEQ. Hence, the contributions of total depositions of atmospheric PCDD/F were only 0.02%. The results indicated that the major sources of PCDD/F for the contaminated soil could be attributed to the pentachlorophenol manufacturing process.     

Distribution patterns of nitroaromatic compounds in the water, suspended particle and sediment of the river in a long-term industrial zone (China)

Nitroaromatic compounds are known to be hazardous to ecological and human health. To assess the status of nitroaromatic compounds contamination in the main rivers in the important industrial bases of the northeastern China, we collected water, suspended particulate matter (SPM) and sediment samples from 28 sites in the Daliao River watershed and analysed them for eight nitroaromatic compounds by gas chromatography. The total concentrations of eight nitrobenzenes in the water column including aqueous and SPM phases ranged from 740 to 15,828 ng L^???1, with a mean concentration of 3,460 ng L^???1. The total concentrations of eight nitrobenzenes in the sediment were 7.47 to 8,185.76 ng g^???1, with a mean concentration of 921.98 ng g^???1, and several times higher than those found from the Yellow River in China. 4-Nitrotoluene was the predominant contaminant in the water and sediment of the three rivers of the Daliao River watershed. 2,6-Dichloro-4-nitroaniline was generally dominant in the SPM. The levels of nitroaromatic compounds were different among different sites in the Daliao River watershed, mainly caused by the distribution of pollution sources. No obvious correlation was found between the total concentrations of eight nitrobenzenes concentrations and TOC or the slit-clay content of the sediments.     

Particulate matter levels in a South American megacity: the metropolitan area of Lima-Callao,Peru

The temporal and spatial trends in the variability of PM₁₀ and PM_2.5 from 2010 to 2015 in the metropolitan area of Lima-Callao, Peru, are studied and interpreted in this work. The mean annual concentrations of PM₁₀ and PM_2.5 have ranges (averages) of 133–45 μg m^?3 (84 μg m^?3) and 35–16 μg m^?3 (26 μg m^?3) for the monitoring sites under study. In general, the highest annual concentrations are observed in the eastern part of the city, which is a result of the pattern of persistent local winds entering from the coast in a south-southwest direction. Seasonal fluctuations in the particulate matter (PM) concentrations are observed; these can be explained by subsidence thermal inversion. There is also a daytime pattern that corresponds to the peak traffic of a total of 9 million trips a day. The PM_2.5 value is approximately 40% of the PM₁₀ value. This proportion can be explained by PM₁₀ re-suspension due to weather conditions. The long-term trends based on the Theil-Sen estimator reveal decreasing PM₁₀ concentrations on the order of ?4.3 and ?5.3% year^?1 at two stations. For the other stations, no significant trend is observed. The metropolitan area of Lima-Callao is ranked 12th and 16th in terms of PM₁₀ and PM_2.5, respectively, out of 39 megacities. The annual World Health Organization thresholds and national air quality standards are exceeded. A large fraction of the Lima population is exposed to PM concentrations that exceed protection thresholds. Hence, the development of pollution control and reduction measures is paramount.     

The impact of ground-level fireworks (13?km long) display on the air quality during the traditional Yanshui Lantern Festival in Taiwan

In this study, the concentrations of CO, non-methane hydrocarbons, NO_X, SO₂, benzene, toluene, ethylbenzene, xylene (BTEX), PM₁₀, and PM_2.5 were continuously monitored before and after the fireworks display during the traditional Lantern Festival from March 2?C7, 2007 in Yanshui Town, Taiwan. Major roads in Yanshui Town were surrounded by fireworks 13 km in length, with the display lasting for 45 min. More than 200 small firecracker towers popped up randomly in town, resulting in exceedingly inhomogeneous air quality until the end of display at 03:00 the next day, March 5. During the fireworks display, the hourly concentration of PM₁₀ and PM_2.5 at Yanshui Primary School reached about 429 and 250 ??g m^???3, respectively, which is 10 times the normal level, and 6 s values even went as high as 1,046 and 842 ??g m^???3, respectively. Similarly, BTEX concentration went up to about five to 10 times its normal value during the fireworks display. As indicated by the distribution of submicron particle sizes, the number of particles with a diameter less than 100 nm increased abruptly during the event period. Metal components with concentrations of more than 10 times higher than the normal value at Yanshui Primary School were Sr, K, Ba, Pb, Al, Mg, and Cu, in sequence. Among water-soluble ions, the content of K^?+?, Mg^2?+?, and Cl^??? increased the most, all of which were related to the materials used in the fireworks. The results of this study indicate that fireworks can cause an abrupt increase in the concentration of trace substances in the air within a short period. Although the risks of these trace substances on public health remain to be further assessed, the study results can be utilized in the management of folk events.     

Concentrations, sources, and exposure profiles of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM10) in the north central part of India

Airborne particulates (PM₁₀) from four different areas within Agra city (a semi-arid region) were collected using respirable dust samplers during the winter season (Nov. 2005–Feb 2006) and were then extracted with methylene chloride using an automated Soxhlet Extraction System (Soxtherm^®). The extracts were analyzed for 17 target polycyclic aromatic hydrocarbons (PAHs) and the heterocycle carbazole. The average concentration of total PAH (TPAH) ranged from 8.04 to 97.93 ng m^???3. The industrial site had the highest TPAH concentration followed by the residential, roadside, and agricultural sites. Indeno(1,2,3-cd)pyrene, benzo(g,h,i)perylene, and benzo(b)fluoranthene were the predominant compounds found in the samples collected from all of the sites. The average B(a)P-equivalent exposure, calculated by using toxic equivalent factors derived from literature and the USEPA, was approximately 7.6 ng m^???3. Source identification using factor analysis identified prominent three, four, four, and four probable factors at industrial, residential, roadside, and agricultural sites, respectively.     

Monitoring of ambient particles and heavy metals in a residential area of Seoul, Korea

In this study, ambient TSP, PM10, and PM2.5 in a residential area located in the northern part of Seoul were monitored every other month for 1 year from April 2005 to February 2006. The monthly average levels of TSP, PM10, and PM2.5 had ranges of 71∼158, 40∼106, and 28∼43 μg/m³, respectively. TSP and PM10 showed highest concentration in April; this seems to be due to Asian dust from China and/or Mongolia. However, the fine particle of PM2.5 showed a relatively constant level during the monitoring period. Heavy metals in PM 10 and PM2.5, such as Cr, As, Cd, Mn, Zn and Pb, were also analysed during the same period. The monthly average concentrations of heavy metal in PM2.5 were Cr:1.9∼22.7 ng/m³; As:0.9∼2.5 ng/m³; Cd: 0.6∼7 ng/m³; Mn:6.1∼22.6 ng/m³; Zn: 38.9∼204.8 ng/m³, and Pb: 21.6∼201.1 ng/m³. For the health risk assessment of heavy metals in ambient particles, excess cancer risks were calculated using IRIS unit risk. As a result, the excess cancer risks of chromium, cadmium, and arsenic were shown to be more than one per million based on the annual concentration of heavy metals, and chromium showed the highest excess cancer risk in ambient particles in Seoul.     

Monitoring of copper level in water and soil samples by using liquid–liquid extraction

A new, simple, sensitive, and selective spectrophotometric method for the determination of copper in water and soil samples has been demonstrated. The method is based on the reaction of Cu(I) with neocuproine (2,9-dimethyl-1, 10-phenanothroline) and extracted with N-phenyl benzimidoylthiourea in chloroform. The value of molar absorptivity of the complex in the term of Cu(I) is 1.45 × 10⁵ L mol^???1 cm^???1 at λ _max 460 nm in chloroform. The detection limit of copper in water and soil is 2 ng mL^???1 and 4 ng g^???1, respectively. The method is free from the interference of the ions commonly found to be associated with the copper determination in water and soil samples. The application of the proposed method has been successfully tested for the determination of copper in different types of water and soil samples.     

Multi-year monitoring of estuarine sediments as ultimate sink for DDT, HCH, and other organochlorinated pesticides in Argentina

Forty-nine superficial sediment samples used in this study were collected from eight sites in the Bahia Blanca Estuary, located in the Buenos Aires Province southwest, Argentina, in a period between April 2005 and March 2009, to assess the concentration levels, spatial and seasonal distribution, and putative input sources of 18 selected organochlorine pesticides (OCs), following UNEP-IAEA procedures. Average concentration levels in sediments ranged between 3.54 and 63.79 ng g^???1, d.w. (mean = 15.99 ng g^???1, d.w.), for ??OCs, and from nondetectable to 8.03 ng g^???1, d.w. (mean = 2.16 ng g^???1, d.w.), and from nondetectable to 3.20 ng g^???1 (mean = 0.97 ng g^???1, d.w.) for hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs), respectively. Principal component analysis allowed the classification of sampling sites according to the main OCs inputs over the estuary. In comparison to other worldwide locations and to the world coastal sediment concentrations range, sediment DDTs and HCHs levels were in the low range; on the opposite, ??OCs average was in the medium range. OCs seasonal distribution was found to be highly correlated with the precipitations seasonality and sowing seasons in the adjacent agriculture fields. In addition, an ecotoxicological risk assessment pointed industrial and agriculture catchment zones with intermediate probability of adverse effects to biota, while the city sewage outfall was classified with none indication of an immediate threat. Data indicated that the estuary sediments were functioning as a sink for persistent OC pesticides (either in use or banned), however, it was found a declining trend on their environmental burden.     

Identification of sources of elevated concentrations of polycyclic aromatic hydrocarbons in an industrial area in Tianjin, China

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were determined by gas chromatography equipped with a mass spectrometry detector in 105 topsoil samples from an industrial area around Bohai Bay, Tianjin in the North of China. Results demonstrated that concentrations of PAHs in 104 soil samples from this area ranged from 68.7 to 5,590 ng g^???1 dry weight with a mean of ∑16PAHs 814 ± 813 ng g^???1, which suggests that there exists mid to high levels of PAH contamination. The concentration of ∑16PAHs in one soil sample from Tianjin Port was exceptionally high (48,700 ng g^???1). Ninety-three of the 105 soil samples were considered to be contaminated with PAHs (>200 ng g^???1), and 25 were heavily polluted (>1,000 ng g^???1). The sites with high PAHs concentration are mainly distributed around chemical industry parks and near highways. Two low molecular weight PAHs, naphthalene and phenanthrene, were the dominant components in the soil samples, which accounted for 22.1% and 10.7% of the ∑16PAHs concentration, respectively. According to the observed molecular indices, house heating in winter, straw stalk combustion in open areas after harvest, and petroleum input were common sources of PAHs in this area, while factory discharge and vehicle exhaust were the major sources around chemical industrial parks and near highways. Biological processes were probably another main source of low molecular weight PAHs.     

Risk assessment due to ingestion of natural radionuclides and heavy metals in the milk samples: a case study from a proposed uranium mining area, Jharkhand

Ingestion of radionuclides and heavy metals through drinking water and food intake represents one of the important pathways for long-term health considerations. Milk and milk products are main constituents of the daily diet. Radionuclides and heavy metals can be apprehended in the ecosystem of the East Singhbhum region which is known for its viable grades of uranium, copper and other minerals. For the risk assessment studies, samples of milk were collected from twelve villages around Bagjata mining area and analysed for U(nat), ²²⁶Ra, ²³⁰Th, ²¹⁰Po, Fe, Mn, Zn, Pb, Cu and Ni. Analysis of the results of the study reveals that the geometric mean of U(nat), ²²⁶Ra, ²³⁰Th and ²¹⁰Po was 0.021, 0.24, 0.23 and 1.08 Bq l^???1, respectively. The ingestion dose was calculated to be 12.34 ??SvY^???1 which is reflecting the natural background dose via the route of ingestion, and much below the 1 mSv limit set in the new ICRP recommendations. The excess lifetime cancer risk was estimated to be 1.72 × 10^???4 which is within the acceptable excess individual lifetime cancer risk value of 1 × 10^???4. The geometric mean of Fe, Mn, Zn, Cu and Ni was 4.91, 0.29, 4.77, 0.56 and 0.48 mgl^???1, respectively; whereas the daily intake was computed to be 0.44, 0.03, 0.43, 0.05 and 0.04 mg/day, respectively. Pb was not detected in any of the samples. The hazard quotient revealed that the intake of the heavy metals through the ingestion of milk does not pose any apparent threat to the local people as none of the HQ of the heavy metals exceeds the limit of 1.     

Mercury accumulation in fish species from the Persian Gulf and in human hair from fishermen

Total and methylmercury concentrations were assessed in muscle and liver of 141 fish samples from the northern part of the Persian Gulf. All fish samples belonged to five different species: grunt, flathead, greasy grouper, tiger-tooth croaker, and silver pomfret. In addition, Hg and methylmercury were analyzed in scalp hair of 19 fishermen living in the same coastal stations of the Persian Gulf and consuming several fish meals a week. Total mercury concentrations in fish muscle and liver ranged from 0.01 to 1.35 μg g^???1 w.w. and from 0.02 to 1.30 μg g^???1 w.w., respectively. In fish muscle, 3% of the Hg concentrations were higher than 0.5 μg g^???1 w.w., which corresponds to the maximum acceptable WHO level, while 9% were in the range of polluted fish (between 0.3 and 0.5 μg g^???1 w.w.). The highest mercury concentrations in fish muscle were observed in flathead fish at Abadan (average of 0.68 μ g g^???1 w.w.). Methylmercury fractions in fish muscle and liver amount to 34–99% (median 64%) and 24–70% (median 43%), respectively. The mean total Hg concentration in the fishermen’s scalp hair amounted to 2.9 ± 2.2 μ g g^???1, with 68% in the form of methylmercury. Ninety-five percent of the Hg levels in the fishermen’s hair were below 10 μ g g^???1, which is the WHO warning limit. In addition, relationships between the mercury levels in hair, on the one hand, and exposure-related factors such as Hg levels in specific fish species, regional differences, and number of fish meals, on the other hand, are discussed. It appears that a significant correlation for example exists between Hg levels human hair and fish muscle or human hair and age and that mean mercury levels in fish muscle and human hair decreased from western (Abadan) to eastern (Abbas port) coastal sites.     

Re-construction of the shut-down PM10 monitoring stations for the reliable assessment of PM10 in Berlin using fuzzy modelling and data transformation

A dense monitoring network is vital for the reliable assessment of PM10 in different parts of an urban area. In this study, a new idea is employed for the re-construction of the 20 shut-down PM10 monitoring stations of Berlin. It endeavours to find the non-linear relationship between the hourly PM10 concentration of both the still operating and the shut-down PM10 monitoring stations by using a fuzzy modelling technique, called modified active learning method (MALM). In addition, the simulations were performed by using not only raw PM10 databases but also log-transformed PM10 databases for skewness reduction. According to the results of hourly PM10 simulation (root mean square error about 13.0 μg/m³, correlation coefficient 0.88), the shut-down stations have been appropriately simulated and the idea of dense monitoring network development by the re-construction of the shut-down stations was realised. The results of simulations using raw and log-transformed databases showed that data transformation has no significant effect on the performance of MALM in the simulation of shut-down PM10 stations. By the combination of the 11 still operating stations and the 20 re-constructed stations, a dense monitoring network was generated for Berlin and was utilised for the calculation of the reliable monthly and mean annual PM10 concentration for five different PM10 zones in Berlin (the suburban-background, urban-background, urban-traffic, rural-background and suburban-traffic areas). The results showed that the mean annual concentration of PM10 at the five zones increased by about 13.0% in 2014 (26.3 μg/m³) in comparison with 2013 (23.3 μg/m³). Furthermore, the mean annual concentration of PM10 in the traffic lanes of the suburban (2013 25.0 μg/m³, 2014 26.9 μg/m³) and urban (2013 27.7 μg/m³, 2014 31.3 μg/m³) areas is about 14 and 20% higher than the PM10 concentration of suburban-background (2013 21.3 μg/m³, 2014 24.5 μg/m³) and urban-background (2013 23.0 μg/m³, 2014 26.1 μg/m³) areas, respectively.     

Selenium in surface and irrigation water in the Kendrick irrigation district, Wyoming

High selenium (Se) concentrations have been found in surface waters in the Kendrick Reclamation Project, Wyoming. Precipitation and irrigation water moving over seleniferous soils are contributing causes, and drought may exacerbate this. This study surveyed Se concentrations and discharges in local surface streams, irrigation drains, and the delivery canal. Sites were sampled monthly and analyzed for Se and total suspended solids (TSS). A completely randomized design with two factors (soil parent material and location, inside or outside irrigation district) was used. Mean Se concentrations were 64 μg L^???1 inside the irrigation district on shale soils, 17 μg L^???1 inside the district off shale soils, 5 μg L^???1 outside the district on shale soils, and 3 μg L^???1 outside the district off shale soils. Correlations between discharge and Se concentrations were generally negative, while correlations between discharge and Se load were generally positive. There was little correlation between load and concentration, and little correlation between TSS and Se. A comparison of Se concentrations in streams and drains showed Se concentrations were significantly higher (p?<?0.001) in streams during the irrigation season, but not in the off-season (p?=?0.515). We conclude that higher discharges decrease Se concentration, but increase load. Conversion from flood to sprinkle irrigation may increase Se concentrations by reducing discharge, but decrease Se loads going into the N. Platte River, and will likely alter the timing and magnitude of flows. Both load and concentration should be considered when implementing Se regulations and standards.     

Assessment of indoor and outdoor particulate air pollution at an urban background site in Iran

The relationship between indoor and outdoor particulate air pollution was investigated at an urban background site on the Payambar Azam Campus of Mazandaran University of Medical Sciences in Sari, Northern Iran. The concentration of particulate matter sized with a diameter less than 1 μm (PM_1.0), 2.5 μm (PM_2.5), and 10 μm (PM₁₀) was evaluated at 5 outdoor and 12 indoor locations. Indoor sites included classrooms, corridors, and office sites in four university buildings. Outdoor PM concentrations were characterized at five locations around the university campus. Indoor and outdoor PM measurements (1-min resolution) were conducted in parallel during weekday mornings and afternoons. No difference found between indoor PM₁₀ (50.1 ± 32.1 μg/m³) and outdoor PM₁₀ concentrations (46.5 ± 26.0 μg/m³), indoor PM_2.5 (22.6 ± 17.4 μg/m³) and outdoor PM_2.5 concentration (22.2 ± 15.4 μg/m³), or indoor PM_1.0 (14.5 ± 13.4 μg/m³) and outdoor mean PM_1.0 concentrations (14.2 ± 12.3 μg/m³). Despite these similar concentrations, no correlations were found between outdoor and indoor PM levels. The present findings are not only of importance for the potential health effects of particulate air pollution on people who spend their daytime over a period of several hours in closed and confined spaces located at a university campus but also can inform regulatory about the improvement of indoor air quality, especially in developing countries.     

Evaluation of levels, sources and distribution of toxic elements in PM10 in a suburban industrial region, Rio de Janeiro, Brazil

The Oswaldo Cruz Foundation Campus (FIOCRUZ), in a suburban region of the city of Rio de Janeiro, was selected as a case study to assess the pollution released from vehicle and industrial facilities in Basin III, the most polluted area of the city. Concentrations of particulate matter (PM10) and trace metals in airborne particles were determined in an intensive field campaign. The samplings were performed every six days for 24 h periods, using a PM10 high volume sampler, from September 2004 to August 2005. PM10 mass concentrations were determined gravimetrically and the metals by ICP-OES. For PM10, the arithmetic mean for the period is 169 ± 42 μg m⁻³ which is 3.4 times the national recommended standard of 50 μg m⁻³. Additionally, 51% of the samplings exceeded the recommended 24 h limit of 150 μg m⁻³. Ca, Mg, Fe, Zn and Al were the metals that presented the higher concentrations. The correlation matrix gave two main clusters and three significant principal components (PC). Both PC1 and PC2 are associated to crustal, vehicular and industrial emissions while PC3 is mainly associated to geological material. Enrichment factors for Zn, Cu, Cd and Pb indicate that for these elements, anthropic sources prevail over natural inputs. PM10 levels showed a good correlation with hospital admissions for respiratory diseases in children and elderly people.     

Demonstrating PM<Subscript>2.5</Subscript> and road-side dust pollution by heavy metals along Thika superhighway in Kenya,sub-Saharan Africa

This study assessed the level of heavy metal in roadside dust and PM_2.5 mass concentrations along Thika superhighway in Kenya. Thika superhighway is one of the busiest roads in Kenya, linking Thika town with Nairobi. Triplicate road dust samples collected from 12 locations were analysed for lead (Pb), chromium (Cr), cadmium (Cd), nickel (Ni), zinc (Zn), and copper (Cu) using atomic absorption spectrophotometry (AAS). PM_2.5 samples were collected on pre-weighed Teflon filters using a BGI personal sampler and the filters were then reweighed. The ranges of metal concentrations were 39–101 μg/g for Cu, 95–262 μg/g for Zn, 9–28 μg/g for Cd, 14–24 μg/g for Ni, 13–30 μg/g for Cr, and 20–80 μg/g for Pb. The concentrations of heavy metals were generally highly correlated, indicating a common anthropogenic source of the pollutants. The results showed that the majority of the measured heavy metals were above the background concentration, and in particular, Cd, Pb, and Zn levels indicated moderate to high contamination. Though not directly comparable due to different sampling timeframes (8 h in this study and 24 h for guideline values), PM_2.5 for all sites exceeds the daily WHO PM_2.5 guidelines of 25 μg/m³. This poses a health risk to people using and working close to Thika superhighway, for example, local residents, traffic police, street vendors, and people operating small businesses. PM_2.5 levels were higher for sites closer to Nairobi which could be attributed to increased vehicular traffic towards Nairobi from Thika. This study provides some evidence of the air pollution problem arising from vehicular traffic in developing parts of the world and gives an indication of the potential health impacts. It also highlights the need for source apportionment studies to determine contributions of anthropogenic emissions to air pollution, as well as long-term sampling studies that can be used to fully understand spatiotemporal patterns in air pollution within developing regions.     

Assessment of environmental radioactivity for Batman, Turkey

The province of Batman, located in southern Anatolia, has a population of approximately 500,000. To our knowledge, there exists no information regarding the environmental radioactivity in this province. Therefore, gamma activity measurements in soil, building materials and water samples and an indoor radon survey have been carried out in the Batman province. The mean activity concentrations of the natural radionuclides (²²⁶Ra, ²³²Th and ⁴⁰K) and a fission product (¹³⁷Cs) were 35 ± 8, 25 ± 10, 274 ± 167 and 12 ± 7 Bq kg^???1, respectively, in the soil samples. The concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in the selected building materials ranged from 18 to 48 Bq kg^???1, 8 to 49 Bq kg^???1 and 68 to 477 Bq kg^???1, respectively. All the calculated radium equivalent (Ra_eq) activity values of the building material samples are lower than the limit of 370 Bq kg^???1, equivalent to a γ-dose of 1.5 mSv year^???1. The activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in tap waters collected from the study area were determined with mean specific activity concentrations of 42 ± 15, 35 ± 9 and 524 ± 190 mBq L^???1, respectively. Indoor radon measurements were made at 95 dwellings in Batman using a CR-39 detector. The radon concentration levels were found to vary from 23 to 145 Bq m^???3. The arithmetic mean of the measured radon concentration levels was found to be 84 Bq m^???3 with a standard deviation value of 23 Bq m^???3. The measurement results obtained in this study did not significantly differ from those taken in other parts of the country. The data generated in this study can be used to determine whether the Batman province is in a normal or high background radiation area and provides a valuable database for future estimations of the impact of radioactive pollution.     

Monsoon-induced changes in the size-fractionated phytoplankton biomass and production rate in the estuarine and coastal waters of southwest coast of India

Changes in the autotrophic pico- (0.2–2 μm), nano- (2–20 μm), and microplankton (>20 μm) biomass (chlorophyll a) and primary production were measured in the estuarine and coastal waters off Cochin, southwest coast of India during the onset and establishment of a monsoon. During this period, the estuary was dominated by nutrient-rich freshwater, whereas the coastal waters were characterized with higher salinity values (>30 psu) and less nutrients. The average surface chlorophyll a concentrations and primary production rates were higher in the estuary (average 13.7 mg m^???3 and 432 mgC m^???3 day^???1) as compared to the coastal waters (5.3 mg m^???3 and 224 mgC m^???3 day^???1). The nanoplankton community formed the major fraction of chlorophyll a and primary production, both in the estuary (average 85 ± SD 8.3% and 81.2 ± SD 3.2%) and the coastal waters (average 73.2 ± SD 17.2% and 81.9 ± 15.7%). Nanoplankton had the maximum photosynthetic efficiency in the coastal waters (average 4.8 ± SD 3.9 mgC mgChl a m^???3 h^???1), whereas in the estuary, the microplankton had higher photosynthetic efficiency (average 7.4 ± 7 mgC mgChl a m^???3 h^???1). The heavy cloud cover and increased water column turbidity not only limit the growth of large-sized phytoplankton in the Cochin estuary and coastal waters but also support the proliferation of nanoplankton community during the monsoon season, even though large variation in nanoplankton chlorophyll a and production exists between these two areas.